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To lead Local Study Team at country level (Philippines) to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with sponsor's Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. The Clinical Lead may perform site monitoring as needed to support the flexible capacity model. The Clinical Lead is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived.